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Dimethylformamide dimethyl acetal → HCID 23152475, 화합물

HRID 1012303
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HRID 1012303 반응식
[C:1]([NH:5][S:6]([C:9]1[CH:14]=[CH:13][C:12]([CH3:15])=[C:11]([N+:16]([O-:18])=[O:17])[CH:10]=1)(=[O:8])=[O:7])([CH3:4])([CH3:3])[CH3:2].CO[CH:21](OC)[N:22]([CH3:24])[CH3:23]>>[C:1]([NH:5][S:6]([C:9]1[CH:14]=[CH:13][C:12](/[CH:15]=[CH:21]/[N:22]([CH3:24])[CH3:23])=[C:11]([N+:16]([O-:18])=[O:17])[CH:10]=1)(=[O:8])=[O:7])([CH3:4])([CH3:2])[CH3:3]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 78373Dimethylformamide dimethyl acetalHCID 2836736HCID 2836736, 화합물

생성물 1

HCID 23152475HCID 23152475, 화합물수율 76.6%

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온도
110 °C

실험 절차

A solution of N-tert-butyl-4-methyl-3-nitrobenzenesulfonamide (5.89 g, 21.6 mmol) in N,N-dimethylformamide dimethyl acetal (10 ml) was stirred with heating at 110° C. for 10 hr. The reaction solvent was evaporated under reduced pressure and diethyl ether was added. The precipitated solid was collected by filtration, washed with diethyl ether and dried in vacuo to give N-tert-butyl-4-((E)-2-dimethylaminovinyl)-3-nitrobenzenesulfonamide (5.41 g, yield 76.6%).

후처리

  1. customThe reaction solvent was evaporated under reduced pressure and diethyl ether
  • additionwas added
  • filtrationThe precipitated solid was collected by filtration
  • washwashed with diethyl ether
  • customdried in vacuo
  • 출처 및 근거

    ORD 기록
    ord-9899ea80ee7746a6a8fdd71093f8e4db
    출처 데이터셋
    uspto-grants-2011_07
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07977331B1

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